US20080119903A1 - Cardiac resynchronization therapy optimization using cardiac activation sequence information - Google Patents

Abstract

Systems and methods provide for pacing a heart to improve pumping efficiency of the heart, such as by producing a cardiac fusion response for patient's subject to cardiac resynchronization therapy. A pacing parameter, such as an A-V delay, V-V delay, lead/electrode configuration or vector, is adjusted and a cardiac signal vector representative of all or a portion of one or more cardiac activation sequences is monitored during pacing parameter adjustment. A change in a characteristic of the cardiac signal vector is detected in response to an adjusted pacing parameter, the change indicative of a cardiac fusion response. A pacing therapy may be delivered to produce the cardiac fusion response using the adjusted pacing parameter.

Description

FIELD OF THE INVENTION
• The present invention relates generally to medical devices that deliver cardiac electrical therapy and, more particularly, to cardiac stimulation devices that optimize cardiac resynchronization therapy using cardiac activation sequence information.
BACKGROUND OF THE INVENTION
• Rhythmic contractions of a healthy heart are normally controlled by the sinoatrial (SA) node which includes specialized cells located in the superior right atrium. The SA node is the normal pacemaker of the heart, typically initiating 60-100 heart beats per minute. When the SA node is pacing the heart normally, the heart is said to be in normal sinus rhythm.
• The heart has specialized conduction pathways in both the atria and the ventricles that enable the rapid conduction of excitation impulses (i.e. depolarizations) from the SA node throughout the myocardium. These specialized conduction pathways conduct the depolarizations from the SA node to the atrial myocardium, to the atrio-ventricular node, and to the ventricular myocardium to produce a coordinated contraction of both atria and both ventricles.
• The conduction pathways synchronize the contractions of the muscle fibers of each chamber as well as the contraction of each atrium or ventricle with the contralateral atrium or ventricle. Without the synchronization afforded by the normally functioning specialized conduction pathways, the heart's pumping efficiency is greatly diminished. Patients who exhibit pathology of these conduction pathways can suffer compromised cardiac output. Cardiac rhythm management devices have been developed that provide pacing stimulation to one or more heart chambers in an attempt to improve the rhythm and coordination of atrial and/or ventricular contractions.
SUMMARY OF THE INVENTION
• The present invention is directed to systems and methods for pacing a heart to improve pumping efficiency of the heart. Embodiments of the present invention are directed to pacing therapies that produce a cardiac fusion response for patient's subject to cardiac resynchronization therapy. Embodiments of the present invention are also directed to optimizing therapy parameters and modifying therapy delivery based on one or more characteristics of a patient's cardiac activation sequence.
• According to embodiments of the present invention, methods for producing a cardiac fusion response involve obtaining a cardiac signal vector associated with all or a portion of one or more cardiac activation sequences. A pacing parameter, such as an A-V delay, V-V delay, lead/electrode configuration or vector, is adjusted and the cardiac signal vector is monitored during pacing parameter adjustment. A change in a characteristic of the cardiac signal vector is detected in response to an adjusted pacing parameter, the change indicative of a cardiac fusion response. A pacing therapy is delivered to produce a cardiac fusion response using the adjusted pacing parameter.
• Detecting the change in the cardiac signal vector characteristic may involve detecting a change in an angle or a magnitude (or both) of the cardiac signal vector. The change in the cardiac signal vector characteristic indicative of the cardiac fusion response may be detected for a range of pacing parameters or parameter values, and the pacing therapy may be delivered using the adjusted pacing parameter falling within the range of pacing parameters or parameter values. Detecting the change in cardiac signal vector characteristic may involve detecting a change between intrinsic cardiac activation and therapy-initiated cardiac activation.
• According to one approach, a change in a cardiac signal vector indicative of intrinsic cardiac activation is detected relative to a baseline. In response to this change in intrinsic cardiac activation, pacing parameter adjustment and detection of a change in the cardiac signal vector characteristic indicative of a fusion response are repeated. The adjusted or updated pacing parameter that produces a fusion response is stored for subsequent pacing therapy delivery. This update process may be initiated automatically or in response to local or remote user input.
• Methods of the present invention may involve detecting a change in a cardiac signal vector indicative of therapy-initiated cardiac activation relative to a first baseline and absence of change in a cardiac signal vector indicative of intrinsic cardiac activation relative to a second baseline. In response to the detected change, the pacing parameter is adjusted to produce the cardiac fusion response for subsequent pacing therapy delivery. Methods may involve accessing a look-up table of pacing parameters pre-established for the patient, such that the pacing parameters of the look-up table, when implemented, produce a cardiac fusion response for the patient. The adjusted pacing parameter may be selected from the look-up table.
• According to other embodiments of the present invention, systems may be implemented to include a plurality of electrodes configured for sensing cardiac electrical activity and energy delivery. A signal processor is coupled to the electrodes and configured to produce a cardiac signal vector associated with all or a portion of one or more cardiac activation sequences. A controller is coupled to the electrodes and the signal processor.
• The controller is configured to adjust a pacing parameter and detect a change in a characteristic of the cardiac signal vector in response to an adjusted pacing parameter, the change indicative of a cardiac fusion response. The controller may be further configured to deliver a pacing therapy to produce the cardiac fusion response using the adjusted pacing parameter. The change in characteristic of the cardiac signal vector detected by the controller may indicate a change between pacing-dominant cardiac activation, fusion, and intrinsic-dominant cardiac activation.
• The controller may be disposed within an implantable housing, a patient-external housing, or distributed in both the implantable and patient-external housing. The signal processor may be disposed within an implantable housing, a patient-external housing, or distributed in both the implantable and patient-external housing. The plurality of electrodes may comprise implantable electrodes, cutaneous electrodes, or a combination of implantable and cutaneous electrodes.
• In some configurations, the controller and the signal processor may be provided in an implantable housing, and the electrodes may comprise implantable electrodes coupled to, or provided on, the housing. In other configuration, the controller and the signal processor may be provided in a patient-external housing, and the electrodes preferably comprise cutaneous electrodes coupled to the housing.
• The controller may be coupled to memory configured to store a look-up table comprising pacing parameters associated with one or both of heart rate and patient condition, the pacing parameters established to produce a cardiac fusion response. The pacing parameters stored in the look-up table may include A-V and V-V delay parameters, electrode/lead configurations, pacing vectors, and other parameters that influence cardiac pacing. The controller may be configured to update the look-up table with updated pacing parameters in response to a change in the cardiac signal vector characteristic indicative of pace-dominant or intrinsic-dominant cardiac activation, the updated pacing parameters established to produce a cardiac fusion response for the patient. The controller may, in response to a change in the cardiac signal vector characteristic indicative of a change in intrinsic-dominant cardiac activation, be configured to update the look-up table with updated baseline values characterizing each of the patient's intrinsic-dominant cardiac activation and pace-dominant cardiac activation.
• The above summary of the present invention is not intended to describe each embodiment or every implementation of the present invention. Advantages and attainments, together with a more complete understanding of the invention, will become apparent and appreciated by referring to the following detailed description and claims taken in conjunction with the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a diagram that illustrates the influence that a pacing parameter has on the patient's cardiac activation sequence in accordance with embodiments of the present invention;
• FIG. 2 is a diagram of various processes associated with pacing parameter optimization in accordance with an embodiment of the present invention;
• FIG. 3 is a diagram of various processes associated with pacing parameter optimization in accordance with another embodiment of the present invention;
• FIGS. 4A and 4B are pictorial diagrams of an electrocardiogram (ECG) waveform for three consecutive heartbeats (FIG. 4A) and a magnified portion of the electrocardiogram (ECG) waveform for the first two consecutive heartbeats (FIG. 4B);
• FIG. 5 is a polar plot of a cardiac signal vector superimposed over a frontal view of a thorax, with the origin of the polar plot located at the AV node of a patient's heart;
• FIG. 6A is a polar plot of cardiac signal vectors showing QRS and P vectors in accordance with the present invention;
• FIG. 6B illustrates polar plots of cardiac signal vectors obtained from selected portions of an electrocardiogram in accordance with the present invention;
• FIG. 7 is a side view of an implantable cardiac device in accordance with the present invention, having at least three electrodes;
• FIG. 8 is a diagram of an implantable cardiac device with leads implanted within a patient's heart, the implantable cardiac device configured to implement algorithms in accordance with embodiments of the present invention; and
• FIG. 9 is a block diagram of various components of a cardiac device (implantable, patient-external or a combination of both) that implements algorithms in accordance with embodiments of the present invention.
• While the invention is amenable to various modifications and alternative forms, specifics thereof have been shown by way of example in the drawings and will be described in detail below. It is to be understood, however, that the intention is not to limit the invention to the particular embodiments described. On the contrary, the invention is intended to cover all modifications, equivalents, and alternatives falling within the scope of the invention as defined by the appended claims.
DETAILED DESCRIPTION OF VARIOUS EMBODIMENTS
• In the following description of the illustrated embodiments, references are made to the accompanying drawings, which form a part hereof, and in which is shown by way of illustration, various embodiments in which the invention may be practiced. It is to be understood that other embodiments may be utilized, and structural and functional changes may be made without departing from the scope of the present invention.
• A medical device implemented according to the present invention may include one or more of the features, structures, methods, or combinations thereof described hereinbelow. For example, a cardiac stimulator may be implemented to include one or more of the advantageous features and/or processes described herein. It is intended that such a stimulator or other implanted or patient-external device need not include all of the features described herein, but may be implemented to include selected features that provide for useful structures and/or functionality. Such a device may be implemented to provide a variety of therapeutic or diagnostic functions.
• A wide variety of cardiac stimulation devices may be configured to implement a cardiac therapy methodology of the present invention. A non-limiting representative list of such devices includes pacemakers, cardiovertors, defibrillators, resynchronizers, and other cardiac monitoring and therapy delivery devices. These devices may be configured with a variety of electrode arrangements, including cutaneous, transvenous, endocardial, and epicardial electrodes (i.e., intrathoracic electrodes), and/or subcutaneous, non-intrathoracic electrodes, such as can, header and/or indifferent electrodes, subcutaneous array electrodes and/or lead electrodes (i.e., non-intrathoracic electrodes).
• Embodiments of the present invention are directed to monitoring and updating characteristics of a patient's cardiac activation sequence during intrinsic cardiac activation (CA_INT) and therapy-initiated cardiac activation (CA_TX). The degree of changes in CA_INTor CA_TXis used to recommend the need for adjustment or re-optimization of therapy parameters. Therapy parameters, such as A-V delay, V-V delay, pacing site, and pacing configuration, can be changed and changes in the patient's cardiac activation sequence monitored. These changes may be used to identify a patient's cardiac fusion response and to recommend parameters that can produce a fusion response. Selection of these therapy parameters can be effected automatically by the therapy delivery device or through user input, such as by use of a local programmer or personal communicator, or remotely via a networked server system, such as a server-based advanced patient management (APM) system. An example of a user is a clinician.
• To improve pumping efficiency in patients subject to cardiac resynchronization therapy (CRT), it is desirable to achieve a certain level of fusion, whereby a pacing pulse effectively merges with an intrinsic response of a heart chamber. Selection of proper therapy parameters of the therapy delivery device that delivers the pacing pulse is critical in order to achieve fusion. Reliable detection of a cardiac fusion response is necessary in order to determine the proper therapy parameters that will produce the desired cardiac fusion response.
• Embodiments of the present invention are directed to improving pumping efficiency in CRT patients by selection of appropriate therapy parameters based on one or more characteristics of the patient's cardiac activation sequence. Embodiments of the present invention are also directed to detection of a cardiac fusion response and storing of therapy parameters that can be used by a therapy delivery device to produce a fusion response during therapy delivery.
• Embodiments of the present invention are further directed to determining changes in cardiac activation sequence characteristics associated with intrinsic and therapy-based cardiac activation. Deviations in intrinsic cardiac activation from an established baseline may be indicative of a change in cardiac condition, such as a change resulting from ischemia, myocardial infarction or remodeling, for example. Detection of such deviations may be used to trigger an alert regarding the cardiac condition change and/or a request to a user that re-optimization of therapy parameters is needed. Detection of such deviations may trigger an automatic re-optimization of therapy parameters.
• Deviations in therapy-based cardiac activation from an established baseline, in the absence of a deviation in intrinsic cardiac activation, are indicative of change in patient condition, such as activity level (e.g., exercise) or posture, for example. Changes in therapy-based cardiac activation may be used to trigger a change in pacing parameters to improve cardiac pumping efficiency in response to changes in such patient dynamics. In response to changed therapy-based cardiac activation characteristics, new therapy parameters may be obtained, such as from a look-up table, and implemented by the therapy delivery device. If new therapy parameters are not available (e.g., not included in the look-up table), a re-optimization procedure may be performed to obtain therapy parameters appropriate for the change in patient dynamics.
• Re-optimization of therapy parameters typically involves the determination of updated (or new) therapy parameters that will improve pumping efficiency in the patient in view of the change in cardiac condition and/or patient dynamics. The updated or new therapy parameters are preferably stored in a look-up table or other data structure for access by the therapy delivery device. If a change in intrinsic cardiac activation is detected, then it is assumed that a pathological change has occurred in the patient's cardiac condition. In this case, a re-optimization procedure is preferably performed to obtain new baselines for both intrinsic and therapy-based cardiac activation. Updated therapy parameters may then be determined that will improve a patient's pumping efficiency, such as by implementing a cardiac resynchronization therapy using therapy parameters that will produce a cardiac fusion response.
• Re-optimization may also involve implementing a pacing site selection procedure, whereby one or more electrodes, temporal sequence, and/or pulse waveform characteristics are selected or modified for delivery of pacing to enhance the contractile function of a heart chamber. Pacing site optimization may be implemented in accordance with methodologies disclosed in commonly owned U.S. patent application Ser. No. 11/479,877 entitled “Selection Of Pacing Sites To Enhance Cardiac Performance,” filed on Jun. 30, 2006 under Attorney Docket No. GDT.246.A1, which is hereby incorporated herein by reference.
• According to embodiments of the present invention, characteristics of all or a portion of one or more cardiac activation sequences are obtained. The characteristics may include timing (durations) and morphology (e.g., extracted morphological features) of P, QRS, T, and/or U waves of the patient's cardiac activation sequence. For example, characteristics such as amplitude (magnitude) and direction of a cardiac signal vector indicative of all or a portion of one or more cardiac activation sequences are obtained. These characteristics are obtained during intrinsic cardiac activation (CA_INT), such as during rest, and during therapy-initiated cardiac activation (CA_TX), such as during delivery of a pacing therapy using therapy parameters optimized in accordance with embodiments of the present invention.
• Baselines for intrinsic and therapy-initiated cardiac activation characteristics are established, such as by trending these characteristics over time. Deviations of the intrinsic and therapy-initiated cardiac activation characteristics from their respective baselines are detected, and the need for re-optimizing therapy parameters is identified. As therapy parameter(s) are systematically changed, the influence of these changed parameter(s) on the patient's cardiac activation sequence is detected or estimated in order to select therapy parameter(s) that can improve a patient's pumping efficiency, such as by selection of therapy parameters that will produce a cardiac fusion response. Therapy parameters may be optimized (i.e., determined or adjusted so that improved pumping efficiency is achieved) by tracking the influence that therapy parameter(s) have on the patient's cardiac activation sequence.
• Turning now toFIG. 1, there is shown a diagram that illustrates the influence that a pacing parameter has on the patient's cardiac activation sequence.FIG. 1 illustrates the change in the angle of acardiac signal vector8 as a function of pacing parameter change, where the cardiac signal vector can represent all or a portion of one or more cardiac activation sequences. The pacing parameter may be an A-V delay, a V-V delay parameter, a lead/electrode configuration or a pacing vector, for example.
• The cardiac signal vector inregion10 ofFIG. 1 indicates pace-only or pace-dominant cardiac activation. The cardiac signal vector inregion12 indicates fused activation or intrinsic-dominant cardiac activation. Until fusion is reached, the pacing activation (region10) dominates the cardiac activation sequence. In the vicinity of fusion, shown inregion14, there is a significant contribution from intrinsic conduction, which results in a significant change in the magnitude and/or direction of the cardiac signal vector.FIG. 1 shows this change in terms of a change in axis angle of thecardiac signal vector8. The amount of change in a characteristic of the cardiac signal vector is patient-dependent. Therefore, a patient-specific threshold for detecting fusion using a deviation in one or more characteristics of the patient's cardiac signal vector may be determined at implant and later updated, such as during regular follow-up visits with a clinician.
• As is shown inFIG. 1, the patient's cardiac fusion response is associated with a transition region orperiod14 between pace-only/pace-dominant and fused activation/intrinsic-dominant cardiac activation. Thisfusion region14 is associated with a range or set of pacing parameters that can produce fusion (e.g., a range of A-V and/or V-V delay parameters, a set of lead/electrode configurations, or set of pacing vectors). Pacing parameter selection may be made to produce “desirable” or a pre-selected degree of fusion. The degree of fusion may be dependent on the degree of patient-dyssynchrony. For example, patients with wide QRS complexes may exhibit a higher degree of fusion, whereas patients with narrower QRS complexes may show a lesser degree of fusion. Once the patient's cardiac fusion response is identified, the pacing parameters that produced the desired fusion response may be stored and used during pacing therapy.
• FIG. 2 is a diagram of various processes associated with pacing parameter optimization in accordance with an embodiment of the present invention. According toFIG. 2, a cardiac signal vector associated with all or a portion of one or more cardiac activation sequences is obtained20. A pacing parameter, such as A-V or V-V delay, lead/electrode configuration or vector, is adjusted22, and the cardiac signal vector monitored24 during pacing parameter adjustment. It is understood that more than one pacing parameter may be adjusted at the same time and the results of such adjustments monitored. Pacing parameter adjustment and monitoring of the cardiac signal vector continue until a change in the cardiac signal vector is detected. If a change in a characteristic (e.g., magnitude or angle) of the cardiac signal vector above a threshold (e.g., patient-dependent threshold) is detected26, such as that indicative of a change from pace-dominant to intrinsic-dominant cardiac activation (or vice-versa), the pacing parameter or pacing parameter range associated with the change (e.g., fusion transition region) is determined28. A pacing therapy may be modified30 by using this pacing parameter(s) to produce a cardiac fusion response.
• FIG. 3 is a diagram of various processes associated with pacing parameter optimization in accordance with another embodiment of the present invention. According toFIG. 3, one or more cardiac activation sequence characteristics are measured40 for intrinsic (CA_INT) and therapy-based (CA_TX) cardiac activation. Baselines for both intrinsic and therapy-based cardiac activation are established, such as by averaging CA_INTand CA_TXcharacteristic values over time.
• If no significant change in CA_INTor CA_TXcharacteristic values is detected, as is tested atdecision block44, the baseline determination processes42 continue. A significant change in a CA_INTor CA_TXcharacteristic values may be determined based on a patient-specific threshold, as discussed previously, or a statistically significant deviation (e.g., ≧3 sigma from standard deviation; ≧x % change) relative to baseline. If a significant change in CA_INTor CA_TXcharacteristic values is detected, then a check is made to determine if the change is a result of a change in the patient's cardiac condition or activity level/posture.
• If a change in a CA_TXcharacteristic value is detected50 with no appreciable change in a CA_INTcharacteristic value, then it is assumed that a change in patient dynamics has been detected. In order to improve cardiac pumping efficiency in view of the change in patient dynamics, one or more therapy parameters may be adjusted to accommodate such chance. According to one approach, a look-up table of therapy parameters pre-established for the patient may be accessed52. The look-up table preferably includes a matrix of heart/pacing rates and associated pacing parameters (A-V and/or V-V delays, lead/electrode configurations, pacing vectors) that were determined to produce a cardiac fusion response for the patient, such as by using the methodology illustrated inFIG. 2. For example, the look-up table may include electrode location and pacing vector information for one or more leads, such as a multi-polar lead, active can electrodes, indifferent electrodes, and subcutaneous electrode arrays, among others.
• The look-up table may include other parameters, such as posture positions/angles and activity levels, for example. Based on changes in patient dynamics (e.g., heart rate, posture, activity level), appropriate therapy parameters may be obtained from the look-up table. Therapy parameter(s) used by the therapy delivery device may be modified56 to include the parameter(s) obtained from the look-up table, and therapy may be delivered to the patient based on the modified therapy parameter(s).
• If a therapy parameter is not available in the look-up table for a given patient dynamic condition, a re-optimization procedure may be performed to determine such unavailable parameter. The methodology illustrated inFIG. 2 may be implemented to determine54 the previously unavailable parameter. For example, the clinician may systematically have the patient exercise and/or orient the patient in various positions while one or more pacing parameters are adjusted to produce a fusion response. Patient dynamic condition parameters and associated therapy parameters may be stored as new or updated data entries in the look-up table.
• An alert may be initiated54 for clinician recognition that look-up table updating is needed, such as by way of a programmer or APM alert. A request for look-up table updating may also be generated and communicated to the clinician via a programmer or APM message. A look-up table update procedure may be initiated automatically by the therapy delivery device or in response to clinician input/instruction.
• If a change in a CA_INTcharacteristic value is detected, as is tested atdecision block60, then it is assumed that a pathological change has occurred in the patient's cardiac condition. A request for, or triggering of, a re-optimization procedure may be initiated62. In response to the trigger or clinician input/instruction, a re-optimization procedure is performed62 to obtain new baseline characteristics for both intrinsic (CA_INT) and therapy-based (CA_TX) cardiac activation. Updated therapy parameters are also determined62, as in a manner discussed above, in view of the pathological change in the patient's cardiac condition. The updated therapy parameters and baseline characteristics for CA_INTand CA_TXare stored64 in the look-up table. The processes depicted inFIG. 3 are then repeated based on the look-up table updates.
• Cardiac activation sequence monitoring and/or tracking according to the present invention preferably employs more than two electrodes of varying location, and possibly of varying configuration. As discussed previously, the electrodes may be cutaneous, subcutaneous or intrathoracic electrodes, or any combination of such electrodes.
• Electrocardiogram (ECG) signals originate from electrophysiological signals propagated through the heart muscle, which provide for the cardiac muscle contraction that pumps blood through the body. A sensed ECG signal is effectively a superposition of all the depolarizations occurring within the heart that are associated with cardiac contraction, along with noise components. The propagation of the depolarizations through the heart may be referred to as a depolarization wavefront. The sequence of depolarization wavefront propagation through the chambers of the heart, providing the sequential timing of the heart's pumping, is designated a cardiac activation sequence.
• Various known approaches may be used to separate activation sequence components of ECG signals, and produce one or more cardiac signal vectors associated with all or a portion of one or more cardiac activation sequences based on the separation. The activation sequence components may be considered as the signal sources that make up the ECG signals, and the signal separation process may be referred to as a source separation process or simply source separation. One illustrative signal source separation methodology useful for producing cardiac signal vectors associated with cardiac activation sequences is designated blind source separation, and is described in greater detail in commonly owned U.S. Published Application No. 2006/0069322, filed Sep. 30, 2004 under U.S. Ser. No. 10/955,397, which is hereby incorporated herein by reference.
• In general, the quality of the electrocardiogram or electrogram sensed from one pair of electrodes of a cardiac therapy device depends on the orientation of the electrodes with respect to the depolarization wavefront produced by the heart. The signal sensed on an electrode bi-pole is the projection of the ECG vector in the direction of the bi-pole. Cardiac activation sequence monitoring and/or tracking algorithms advantageously exploit the strong correlation of signals from a common origin (the heart) across spatially distributed electrodes.
• Referring toFIGS. 4A and 4B, anECG waveform100 describes the activation sequence of a patient's heart as recorded, for example, by a bi-polar cardiac sensing electrode. The graph ofFIG. 4A illustrates an example of theECG waveform100 for three heartbeats, denoted as afirst heartbeat110, asecond heartbeat120, and athird heartbeat130.FIG. 4B is a magnified view of the first twoheartbeats110,120 of the ECG waveform identified bybracket4B inFIG. 4A.
• Referring to thefirst heartbeat110, the portion of the ECG waveform representing depolarization of the atrial muscle fibers is referred to as a P-wave112. Depolarization of the ventricular muscle fibers is collectively represented by aQ114,R116, andS118 waves of theECG waveform100, typically referred to as the QRS complex, which is a well-known morphological feature of electrocardiograms. Finally, the portion of the waveform representing repolarization of the ventricular muscle fibers is known as a T-wave119. Between contractions, the ECG waveform returns to an isopotential level.
• The sensedECG waveform100 illustrated inFIGS. 4A and 4B is typical of a far-field ECG signal, effectively a superposition of all the depolarizations occurring within the heart that result in contraction. TheECG waveform100 may also be obtained indirectly, such as by using a signal separation methodology.
• FIG. 5 illustrates a convenient reference for describing cardiac signal vectors associated with a depolarization wavefront.FIG. 5 is apolar plot200 of acardiac vector240 superimposed over a frontal view of athorax220, with the origin of the polar plot located at a patient'sheart250, specifically, the atrioventricular (AV) node of theheart250. Theheart250 is a four-chambered pump that is largely composed of a special type of striated muscle, called myocardium. Two major pumps operate in the heart, and they are aright ventricle260, which pumps blood into pulmonary circulation, and aleft ventricle270, which pumps blood into systemic circulation. Each of these pumps is connected to its associated atrium, called aright atrium265 and aleft atrium275.
• Thecardiac vector240 is describable as having an angle, in degrees, about a circle of thepolar plot200, and having a magnitude, illustrated as a distance from the origin of the tip of thecardiac vector240. Thepolar plot200 is divided into halves by a horizontal line indicating 0 degrees on the patient's left, and +/−180 degrees on the patient's right, and further divided into quadrants by a vertical line indicated by −90 degrees at the patient's head and +90 degrees on the bottom. Thecardiac vector240 is projectable onto the two-dimensional plane designated by thepolar plot200.
• Thecardiac vector240 is a measure of all or a portion of the projection of a heart's activation sequence onto thepolar plot200. The heart possesses a specialized conduction system that ensures, under normal conditions, that the overall timing of ventricular and atrial pumping is optimal for producing cardiac output, the amount of blood pumped by the heart per minute. The normal pacemaker of the heart is a self-firing unit located in the right atrium called the sinoatrial node. The electrical depolarization generated by this structure activates contraction of the two atria. The depolarization wavefront then reaches the specialized conduction system using conducting pathways within and between the atria. The depolarization is conducted to the atrioventricular node, and transmitted down a rapid conduction system composed of the right and left bundle branches, to stimulate contraction of the two ventricles.
• Thecardiac vector240 may be, for example, associated with the entire cardiac cycle, and describe the mean magnitude and mean angle of the cardiac cycle. Referring now toFIG. 6A, apolar plot300 is illustrated of separate portions of the cardiac cycle that may make up thecardiac vector240 ofFIG. 5. As is illustrated inFIG. 6A, aQRS vector310 and aP vector320 are illustrated having approximately 60 degree and 30 degree angles, respectively. TheQRS vector310 may also be referred to as the QRS axis, and changes in the direction of the QRS vector may be referred to as QRS axis deviations.
• TheQRS vector310 represents the projection of the mean magnitude and angle of the depolarization wavefront during the QRS portion of the cardiac cycle onto thepolar plot300. TheP vector320 represents the projection of the mean magnitude and angle of the depolarization wavefront during the P portion of the cardiac cycle onto thepolar plot300. The projection of any portion of the depolarization wavefront (e.g., P, QRS, T, U) may be represented as a vector on thepolar plot300.
• Further, any number of cardiac cycles may be combined to provide a statistical sample that may be represented by a vector as a projection onto thepolar plot300. Likewise, portions of the cardiac cycle over multiple cardiac cycles may also be combined, such as combining a weighted summation of only the P portion of the cardiac cycle over multiple cardiac cycles, for example.
• Referring now toFIGS. 4A through 6A, the first, second, and thirdcardiac cycles110,120, and130 may be analyzed using a window140 (FIG. 4A) applied concurrently to signals sensed by three or more cardiac sense electrodes. The ECG waveform signals100 from all the sense electrodes, during thewindow140, may be provided to a signal processor. The signal processor may then perform a source separation or other operation that provides the cardiac vector240 (FIG. 5). Thecardiac vector240 then represents the orientation and magnitude of the cardiac vector that is effectively an average over all threecardiac cycles110,120, and130.
• Other windows are also useful. For example, awindow150 and awindow160 may provide each full cardiac cycle, such as thecardiac cycle120 and thecardiac cycle130 illustrated inFIG. 4A, to a controller for analysis. Thewindows150,160 may be useful for beat-to-beat analysis, where the angle, magnitude, or other useful parameter from the separatedcardiac vector240 is compared between consecutive beats, or trended, for example.
• Examples of other useful windows include a P-window152, aQRS window154, and an ST window155 (FIG. 4A) that provide within-beat vector analysis capability, such as by providing the P-vector320 and the QRS-vector310 illustrated inFIG. 6A. Providing a P-window162 and/or a QRS-window164, and/or anST window165 to subsequent beats, such as to the consecutivecardiac cycle130 illustrated inFIG. 4A, provides for subsequent separations that may provide information for tracking and monitoring changes and/or trends of windowed portions of the cardiac cycle or statistical samples of P, QRS, or T waves over more than 1 beat.
• Referring now toFIG. 6B, polar plots of cardiac vectors obtained from selected portions of an electrocardiogram are illustrated. In general, it may be desirable to define one or more detection windows associated with particular segments of a given patient's cardiac cycle. The detection windows may be associated with cardiac signal features, such as P, QRS, ST, and T wave features, for example. The detection windows may also be associated with other portions of the cardiac cycle that change in character as a result of changes in the pathology of a patient's heart. Such detection windows may be defined as fixed or triggerable windows.
• Detection windows may include unit step functions to initiate and terminate the window, or may be tapered or otherwise initiate and terminate using smoothing functions such as Bartlett, Bessel, Butterworth, Hanning, Hamming, Chebyshev, Welch, or other functions and/or filters. The detection windows associated with particular cardiac signal features or segments may have widths sufficient to sense cardiac vectors resulting from normal or expected cardiac activity. Aberrant or unexpected cardiac activity may result in the failure of a given cardiac vector to fall within a range indicative of normal cardiac behavior. Detection of a given cardiac vector beyond a normal range (or relative to a baseline) may trigger one or more operations, such as therapy parameter re-optimization discussed above, and may further involve increased monitoring or diagnostic operations, therapy delivery, patient or physician alerting, communication of warning and/or device/physiological data to an external system (e.g., advanced patient management system) or other responsive operation.
• AnECG signal305 is plotted inFIG. 6B as asignal amplitude350 on the ordinate versus time on the abscissa. One cardiac cycle is illustrated. The P portion of theECG signal305 may be defined using a P-window335 that opens at atime336 and closes at atime337. A source separation performed on the ECG signal305 within the P-window335 produces theP vector310 illustrated on apolar plot330. The angle of theP vector310 indicates the angle of the vector summation of the depolarization wavefront during the time of the P-window335 for theECG signal305.
• The ST portion of theECG signal305 may be defined using an ST-window345 that opens at atime346 and closes at atime347. A source separation or other appropriate operation performed on the ECG signal305 within the ST-window345 produces theST vector350 illustrated on apolar plot340. The angle of theST vector350 indicates the angle of the vector summation of the depolarization wavefront during the time of the ST-window345 for theECG signal305. TheP vector310,ST vector350 or other cardiac signal vector may be acquired as baselines, for future comparisons. As discussed above, detection of a cardiac signal vector characteristic beyond a predetermined baseline or threshold may trigger one or more responsive operations, such as re-optimization of intrinsic and therapy-based cardiac activation sequence characteristics and therapy parameters.
• FIG. 7 is a top view of an implantabletherapy delivery device782 in accordance with an embodiment of the present invention, having at least three electrodes. Although multiple electrodes are illustrated inFIG. 7 as located on the can, typically the can includes one electrode, and other electrodes are coupled to the can using a lead. Thetherapy delivery device782 shown in the embodiment illustrated inFIG. 7 includes afirst electrode781a, asecond electrode781b, and athird electrode781cprovided with acan703. Thetherapy delivery device782 is configured to detect and record cardiac activity. Thetherapy delivery device782 is also configured to delivery a cardiac electrical therapy, such as cardiac resynchronization therapy.
• The can703 is illustrated as incorporating aheader789 that may be configured to facilitate removable attachment between one or more leads and thecan703. The can703 may include any number of electrodes positioned anywhere in or on thecan703, such asoptional electrodes781d,781e,781f, and781g. Each electrode pair provides one vector available for the sensing of ECG signals, and may also be configured for therapeutic energy delivery.
• Referring now toFIG. 8, there is shown a cardiac rhythm management (CRM) system that may be used to implement a cardiac therapy and optimization methodology in accordance with the present invention. The CRM system inFIG. 8 includes a pacemaker/defibrillator800 enclosed within a housing and coupled to alead system802. The housing and/or header of the pacemaker/defibrillator800 may incorporate one or more can orindifferent electrodes808,809 used to provide electrical stimulation energy to the heart and/or to sense cardiac electrical activity. The pacemaker/defibrillator800 may utilize all or a portion of the device housing as acan electrode808. The pacemaker/defibrillator800 may include anindifferent electrode809 positioned, for example, on the header or the housing of the pacemaker/defibrillator800. If the pacemaker/defibrillator800 includes both a can electrode808 and anindifferent electrode809, theelectrodes808,809 typically are electrically isolated from each other.
• Thelead system802 is used to detect cardiac electrical signals produced by the heart and to provide electrical energy to the heart under certain predetermined conditions to treat cardiac arrhythmias. Thelead system802 may include one or more electrodes used for pacing, sensing, and/or defibrillation. In the embodiment shown inFIG. 8, the lead system602 includes an intracardiac right ventricular (RV)lead system804, an intracardiac right atrial (RA)lead system805, and an intracardiac left ventricular (LV)lead system806. An extracardiac left atrial (LA)lead system807 is employed.
• The CRM system illustrated inFIG. 8 is configured for biventricular or biatrial pacing. Thelead system802 ofFIG. 8 illustrates one embodiment that may be used in connection with the cardiac therapy and optimization processes described herein. Other leads and/or electrodes may additionally or alternatively be used. For example, the CRM system may pace multiple sites in one cardiac chamber via multiple electrodes within the chamber. This type of multisite pacing may be employed in one or more of the right atrium, left atrium, right ventricle or left ventricle. Multisite pacing in a chamber may be used for example, to increase the power and or synchrony of cardiac contractions of the paced chamber.
• Thelead system802 may include intracardiac leads804,805,806 implanted in a human body with portions of the intracardiac leads804,805,806 inserted into a heart. The intracardiac leads804,805,806 include various electrodes positionable within the heart for sensing electrical activity of the heart and for delivering electrical stimulation energy to the heart, for example, pacing pulses and/or defibrillation shocks to treat various arrhythmias of the heart.
• As illustrated inFIG. 8, thelead system802 may include one or more extracardiac leads807 havingelectrodes815,818, e.g., epicardial electrodes, positioned at locations outside the heart for sensing and pacing one or more heart chambers. In some configurations, the epicardial electrodes may be placed on or about the outside of the heart and/or embedded in the myocardium from locations outside the heart.
• The rightventricular lead system804 illustrated inFIG. 8 includes an SVC-coil816, an RV-coil814, an RV-ring electrode811, and an RV-tip electrode812. The rightventricular lead system804 extends through the right atrium and into the right ventricle.
• In particular, the RV-tip electrode812, RV-ring electrode811, and RV-coil electrode814 are positioned at appropriate locations within the right ventricle for sensing and delivering electrical stimulation pulses to the heart. The SVC-coil816 is positioned at an appropriate location within the right atrium chamber of the heart or a major vein leading to the right atrial chamber.
• In one configuration, the RV-tip electrode812 referenced to thecan electrode808 may be used to implement unipolar pacing and/or sensing in the right ventricle. Bipolar pacing and/or sensing in the right ventricle may be implemented using the RV-tip812 and RV-ring811 electrodes. In yet another configuration, the RV-ring811 electrode may optionally be omitted, and bipolar pacing and/or sensing may be accomplished using the RV-tip electrode812 and the RV-coil814, for example. The rightventricular lead system804 may be configured as an integrated bipolar pace/shock lead. The RV-coil814 and the SVC-coil816 are defibrillation electrodes.
• Theleft ventricular lead806 includes an LVdistal electrode813 and an LVproximal electrode817 located at appropriate locations in or about the left ventricle for pacing and/or sensing the left ventricle. Theleft ventricular lead806 may be guided into the right atrium of the heart via the superior vena cava. From the right atrium, theleft ventricular lead806 may be deployed into the coronary sinus ostium, the opening of thecoronary sinus850. Thelead806 may be guided through thecoronary sinus850 to a coronary vein of the left ventricle. This vein is used as an access pathway for leads to reach the surfaces of the left ventricle which are not directly accessible from the right side of the heart. Lead placement for theleft ventricular lead806 may be achieved via subclavian vein access and a preformed guiding catheter for insertion of theLV electrodes813,817 adjacent to the left ventricle.
• Unipolar pacing and/or sensing in the left ventricle may be implemented, for example, using the LV distal electrode referenced to thecan electrode808. The LVdistal electrode813 and the LVproximal electrode817 may be used together as bipolar sense and/or pace electrodes for the left ventricle. Thelead system802 in conjunction with the pacemaker/defibrillator800 may provide bradycardia pacing therapy to maintain a hemodynamically sufficient heart rate. Theleft ventricular lead806 and theright ventricular lead804 and/or the right atrial lead and the left atrial lead may be used to provide cardiac resynchronization therapy such that the ventricles and/or atria of the heart are paced substantially simultaneously or in phased sequence separated by an interventricular or interatrial pacing delay, to provide enhanced cardiac pumping efficiency for patients suffering from heart failure.
• The rightatrial lead805 includes a RA-tip electrode856 and an RA-ring electrode854 positioned at appropriate locations in the right atrium for sensing and pacing the right atrium. In one configuration, the RA-tip856 referenced to thecan electrode808, for example, may be used to provide unipolar pacing and/or sensing in the right atrium. In another configuration, the RA-tip electrode856 and the RA-ring electrode854 may be used to effect bipolar pacing and/or sensing.
• Referring now toFIG. 9, there is shown a block diagram of an embodiment of atherapy delivery system900 suitable for implementing cardiac therapy and optimization methodologies of the present invention.Therapy delivery system900 may be incorporated in a patient-implantable therapy device, such as those described above, or in a patient-external therapy device or system.Therapy delivery system900 may also be configured such that one or more components or functions are distributed between implantable and patient-external therapy devices. For example, one or more of control, signal processing, sensing, and energy delivery may be implemented using both implantable and patient-external devices and/or processes.
• FIG. 9 shows atherapy delivery system900 divided into functional blocks. It is understood by those skilled in the art that there exist many possible configurations in which these functional blocks can be arranged. The example depicted inFIG. 9 is one possible functional arrangement. Other arrangements are also possible. For example, more, fewer or different functional blocks may be used to describe a cardiac system suitable for implementing cardiac therapy and optimization processes of the present invention. In addition, although thetherapy delivery system900 depicted inFIG. 9 contemplates the use of a programmable microprocessor-based logic circuit, other circuit implementations may be utilized.
• Thetherapy delivery system900 includes acontrol processor940 capable of controlling the delivery of pacing pulses or, if so configured, defibrillation shocks to the right ventricle, left ventricle, right atrium and/or left atrium. Thepacing therapy circuitry930 may be configured to generate pacing pulses for treating bradyarrhythmia, for example, or for synchronizing the contractions of contralateral heart chambers using biatrial and/or biventricular pacing.
• Thetherapy delivery system900 includes a cardiacactivation sequence processor915 coupled to sense/detection circuitry910. The cardiacactivation sequence processor915 is configured to produce a cardiac signal vector of a type described hereinabove. Thecontrol processor940 is preferably configured to perform the baseline generation and comparison operations discussed above for intrinsic and therapy-based cardiac activation sequence characteristics, and to optimize therapy parameters as previously discussed. Thecontrol processor940 also interacts with a therapy parameter look-up table920 in a manner previously described.
• Thetherapy delivery system900 may also include arrhythmia discrimination circuitry (not shown) configured to classify cardiac rhythms, such as by use of rate-based and/or morphological-based algorithms operating on detected cardiac signals. The arrhythmia discrimination circuitry typically operates to detect atrial and/or ventricular tachyarrhythmia or fibrillation using a multiplicity of discrimination algorithms. Under control of thecontrol processor940, the pacing/cardioversion/defibrillation circuitry935 is capable of generating high energy shocks to terminate the tachyarrhythmia episodes (e.g., antitachycardia pacing (ATP), cardioversion, and defibrillation therapies), as determined by the arrhythmia discriminator circuitry.
• Pacingtherapy circuitry930 is configured to control pacing pulse generation in accordance with a variety of pacing modes and therapies, including resynchronization therapies. Pacingtherapy circuitry930 is also configured to generate pacing pulses to implement cardiac therapy and optimization processes described hereinabove.
• The pacing pulses and/or defibrillation shocks are delivered via multiplecardiac electrodes905 electrically coupled to a heart and disposed at multiple locations on the skin or within, on, or about the heart. One ormore electrodes905 may be disposed over, in, on, or about each heart chamber or at multiple sites of one heart chamber. Theelectrodes905 are coupled to switchmatrix925 circuitry that is used to selectively couple theelectrodes905 to thesense circuitry910 and thetherapy circuitry930,935.
• Thetherapy delivery system900 is typically powered by an electrochemical battery (not shown). Amemory945 stores data (electrograms from multiple channels, timing data, etc.) and program commands used to implement the cardiac pacing therapies, rhythm discrimination if applicable, and therapy optimization processes described herein along with other features. Data and program commands may be transferred between thetherapy delivery system900 and a patient-external device955 via telemetry-basedcommunications circuitry950.
• The patient-external device955 may be implemented as a programmer, an APM system or other external computational resource. Adisplay957 of a user interface of the patient-external device955 is typically provided to facilitate user interaction with the patient-external device955 and the cardiac therapy device. Data transferred from the cardiac therapy device to the patient-external device955 may be organized in a manner useful for presentation to a clinician.
• A user interface may be coupled to the APM system allowing a physician to remotely monitor cardiac functions, as well as other patient conditions, and to interact with a cardiac therapy device in a manner discussed above. The user interface may be used by the clinician to access information available via the APM system. The clinician may also enter information via the user interface for setting up the pacing output configuration functionality and optimizing pacing therapies. For example, the clinician may select particular sensors, hemodynamic status indicators, indicator levels or sensitivities, and/or electromechanical parameters. Methods, structures, and/or techniques described herein, may incorporate various APM related methodologies, including features described in one or more of the following references: U.S. Pat. Nos. 6,221,011; 6,270,457; 6,277,072; 6,280,380; 6,312,378; 6,336,903; 6,358,203; 6,368,284; 6,398,728; and 6,440,066, which are hereby incorporated herein by reference.
• The components, functionality, and structural configurations depicted herein are intended to provide an understanding of various features and combination of features that may be incorporated in an implantable or patient-external cardiac therapy device, such as a pacemaker or pacemaker/defibrillator. It is understood that a wide variety of cardiac monitoring and/or stimulation device configurations are contemplated, ranging from relatively sophisticated to relatively simple designs. As such, particular cardiac device configurations may include particular features as described herein, while other such device configurations may exclude particular features described herein.
• Various modifications and additions can be made to the preferred embodiments discussed hereinabove without departing from the scope of the present invention. Accordingly, the scope of the present invention should not be limited by the particular embodiments described above, but should be defined only by the claims set forth below and equivalents thereof.

Claims (25)

1. A method of pacing a heart to produce a fusion response, comprising:

obtaining a cardiac signal vector associated with all or a portion of one or more cardiac activation sequences;

adjusting one or more pacing parameters and monitoring the cardiac signal vector during pacing parameter adjustment;

detecting a change in a characteristic of the cardiac signal vector in response to the one or more adjusted pacing parameters, the change indicative of a cardiac fusion response; and

delivering a pacing therapy to produce the cardiac fusion response using the one or more adjusted pacing parameters.

2. The method ofclaim 1, wherein the one or more pacing parameters comprises at least an A-V delay parameter.

3. The method ofclaim 1, wherein the one or more pacing parameter comprises at least a V-V delay parameter.

4. The method ofclaim 1, wherein the one or more pacing parameter comprises at least one of a pacing lead configuration, a pacing electrode configuration, or a pacing vector.

5. The method ofclaim 1, wherein detecting the change in the cardiac signal vector characteristic comprises a change in an angle of the cardiac signal vector.

6. The method ofclaim 1, wherein detecting the change in the cardiac signal vector characteristic comprises a change in a magnitude of the cardiac signal vector.

7. The method ofclaim 1, wherein the change in the cardiac signal vector characteristic indicative of the cardiac fusion response is detected for a range of pacing parameter values or a set of pacing parameters, and the pacing therapy is delivered using the adjusted pacing parameter falling within the range of pacing parameter values or selected from the set of pacing parameters.

8. The method ofclaim 1, wherein detecting the change in cardiac signal vector characteristic comprises detecting a change in one or both of intrinsic cardiac activation and therapy-initiated cardiac activation.

9. The method ofclaim 1, further comprising:

detecting a change in a cardiac signal vector indicative of intrinsic cardiac activation relative to a baseline;

repeating the obtaining, adjusting, and detecting processes in response to the detected change from baseline; and

storing the adjusted pacing parameter for subsequent pacing therapy delivery.

10. The method ofclaim 9, wherein the repeating and storing processes are initiated in response to local or remote user input.

11. The method ofclaim 9, wherein the repeating and storing processes are initiated automatically.

12. The method ofclaim 1, further comprising:

detecting a change in a cardiac signal vector indicative of therapy-initiated cardiac activation relative to a first baseline and absence of change in a cardiac signal vector indicative of intrinsic cardiac activation relative to a second baseline; and

in response to the detected change, adjusting the pacing parameter to produce the cardiac fusion response for subsequent pacing therapy delivery.

13. The method ofclaim 12, further comprising accessing a look-up table of pacing parameters established by prior implementation of the obtaining, adjusting, and detecting processes, the adjusted pacing parameter selected from the look-up table.

14. The method ofclaim 1, wherein the pacing therapy comprises a cardiac resynchronization therapy.

15. A system, comprising:

a plurality of electrodes configured for at least sensing cardiac electrical activity and energy delivery;

a signal processor coupled to the electrodes and configured to produce a cardiac signal vector associated with all or a portion of one or more cardiac activation sequences; and

a controller coupled to the electrodes and the signal processor, the controller configured to adjust a pacing parameter and detect a change in a characteristic of the cardiac signal vector in response to an adjusted pacing parameter, the change indicative of a cardiac fusion response.

16. The system ofclaim 15, wherein the controller is configured to deliver a pacing therapy to produce the cardiac fusion response using the adjusted pacing parameter.

17. The system ofclaim 15, wherein the controller is disposed within an implantable housing, a patient-external housing, or distributed in both the implantable and patient-external housing.

18. The system ofclaim 15, wherein the signal processor is disposed within an implantable housing, a patient-external housing, or distributed in both the implantable and patient-external housing.

19. The system ofclaim 15, wherein the plurality of electrodes comprise implantable electrodes, cutaneous electrodes, or a combination of implantable and cutaneous electrodes.

20. The system ofclaim 15, further comprising an implantable housing, wherein the controller and the signal processor are provided in the housing, and the electrodes comprise implantable electrodes coupled to, or provided on, the housing.

21. The system ofclaim 15, further comprising a patient-external housing, wherein the controller and the signal processor are provided in the housing, and the electrodes comprise cutaneous electrodes coupled to the housing.

22. The system ofclaim 15, wherein the change in characteristic of the cardiac signal vector indicates a change between therapy-initiated cardiac activation, fusion, and intrinsic cardiac activation.

23. The system ofclaim 15, wherein the controller is coupled to memory, the memory configured to store a look-up table comprising pacing parameters associated with one or both of heart rate and patient condition, the pacing parameters established to produce a cardiac fusion response.

24. The system ofclaim 23, wherein the controller is configured to update the look-up table with updated pacing parameters in response to a change in the cardiac signal vector characteristic indicative of therapy-initiated or intrinsic cardiac activation, the updated pacing parameters established to produce a cardiac fusion response for the patient.

25. The system ofclaim 23, wherein the controller, in response to a change in the cardiac signal vector characteristic indicative of a change in intrinsic cardiac activation, is configured to update the look-up table with updated baselines characterizing each of the patient's intrinsic cardiac activation and therapy-initiated cardiac activation.

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